Agrobacterium tumefaciens Gene Transfer: How a Plant Pathogen Hacks the Nuclei of Plant and Nonplant Organisms

被引:46
|
作者
Bourras, Salim [1 ]
Rouxel, Thierry [1 ]
Meyer, Michel [1 ]
机构
[1] INRA, AgroParisTech BIOGER, UMR 1290, F-78850 Thiverval Grignon, France
关键词
DOUBLE-STRAND BREAKS; T-DNA INTEGRATION; RNA-POLYMERASE-II; FUNGUS LEPTOSPHAERIA-MACULANS; NUCLEOTIDE EXCISION-REPAIR; IV SECRETION SYSTEMS; GENOME-WIDE ANALYSIS; CROWN-GALL TUMORS; F-BOX PROTEIN; MEDIATED TRANSFORMATION;
D O I
10.1094/PHYTO-12-14-0380-RVW
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Agrobacterium species are soilborne gram-negative bacteria exhibiting predominantly a saprophytic lifestyle. Only a few of these species are capable of parasitic growth on plants, causing either hairy root or crown gall diseases. The core of the infection strategy of pathogenic Agrobacteria is a genetic transformation of the host cell, via stable integration into the host genome of a DNA fragment called T-DNA. This genetic transformation results in oncogenic reprogramming of the host to the benefit of the pathogen. This unique ability of interkingdom DNA transfer was largely used as a tool for genetic engineering. Thus, the artificial host range of Agrobacterium is continuously expanding and includes plant and nonplant organisms. The increasing availability of genomic tools encouraged genome-wide surveys of T-DNA tagged libraries, and the pattern of T-DNA integration in eukaryotic genomes was studied. Therefore, data have been collected in numerous laboratories to attain a better understanding of T-DNA integration mechanisms and potential biases. This review focuses on the intranuclear mechanisms necessary for proper targeting and stable expression of Agrobacterium oncogenic T-DNA in the host cell. More specifically, the role of genome features and the putative involvement of host's transcriptional machinery in relation to the T-DNA integration and effects on gene expression are discussed. Also, the mechanisms underlying T-DNA integration into specific genome compartments is reviewed, and a theoretical model for T-DNA intranuclear targeting is presented.
引用
收藏
页码:1288 / 1301
页数:14
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